Fig. 3.
Fig. 3. Pulse-chase analysis of metabolically labeled late erythroblasts. Late erythroblasts were labeled with [35S]methionine for 60 minutes and then chased with unlabeled methionine for 16 hours. Plasma membranes isolated from unchased and chased cells were extracted with C12E8. (A) The C12E8extracts were subjected to size exclusion HPLC. (B) C12E8-insoluble pellets (P) and -soluble supernatants (S) were immunoprecipitated with anti–band 3 antibodies. The immunoprecipitates were analyzed by SDS-PAGE and the gels were processed for fluorography. (C) The autoradiograms shown in B were scanned and the area under each peak integrated (the autoradiograms for the 2-hour chase period are not shown). Band 3 dimers synthesized before the chase were stable and did not associate to form tetramers during the 16-hour chase period.

Pulse-chase analysis of metabolically labeled late erythroblasts. Late erythroblasts were labeled with [35S]methionine for 60 minutes and then chased with unlabeled methionine for 16 hours. Plasma membranes isolated from unchased and chased cells were extracted with C12E8. (A) The C12E8extracts were subjected to size exclusion HPLC. (B) C12E8-insoluble pellets (P) and -soluble supernatants (S) were immunoprecipitated with anti–band 3 antibodies. The immunoprecipitates were analyzed by SDS-PAGE and the gels were processed for fluorography. (C) The autoradiograms shown in B were scanned and the area under each peak integrated (the autoradiograms for the 2-hour chase period are not shown). Band 3 dimers synthesized before the chase were stable and did not associate to form tetramers during the 16-hour chase period.

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